Oxygen scavengers, compositions comprising the scavengers, and articles made from the compositions

ABSTRACT

The disclosure relates to oxygen scavenging molecules, compositions, methods of making the compositions, articles prepared from the compositions, and methods of making the articles. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority to co-pending U.S.utility patent application Ser. No. 13/889,133, filed May 7, 2013, whichapplication claims the benefit of priority to U.S. utility patentapplication Ser. No. 12/945,355, filed Nov. 12, 2010 (now U.S. Pat. No.8,450,398), which application claims the benefit of priority to U.S.provisional patent application Ser. No. 61/261,219, filed Nov. 13, 2009.The entire disclosure of each of these patent applications isincorporated by reference herein.

BACKGROUND

Many polymers used in packaging materials and other articles arepermeable to oxygen. When oxygen permeates a polymeric composition orarticle, it can cause oxidative damage to the contents of the package.It is therefore desirable for certain polymer compositions and articlesto have oxygen scavenging capability, such that when oxygen permeatesthe composition or article, oxidative damage can be mitigated.

It is known in the art to include an oxygen scavenger in the packagingstructure for the protection of oxygen sensitive materials. Suchscavengers are believed to react with oxygen that is trapped in thepackage or that permeates from outside of the package, thus extending tolife of package contents. These packages include films, bottles,containers, and the like. Food, beverages (such as beer and fruitjuices), cosmetics, medicines, and the like are particularly sensitiveto oxygen exposure and require high barrier properties to oxygen topreserve the freshness of the package contents and avoid changes inflavor, texture and color.

Therefore, a need exists for compounds and compositions having improvedoxygen scavenging capacity. These needs and other needs are satisfied bythe present invention.

SUMMARY

In accordance with the purpose(s) of the invention, as embodied andbroadly described herein, the invention, in one aspect, relates tooxygen scavenging molecules, compositions comprising the molecules, andarticles prepared from the compositions.

Also disclosed are polymer compositions comprising the disclosed oxygenscavenging molecules.

Also disclosed are articles prepared from the disclosed polymers andcompositions.

Also disclosed are methods of making oxygen scavenging molecules andpolymer compositions comprising the disclosed oxygen scavengingmolecules.

Also disclosed are the products of the disclosed methods.

Additional advantages of the invention will be set forth in part in thedescription which follows, and in part will be obvious from thedescription, or can be learned by practice of the invention. Theadvantages of the invention will be realized and attained by means ofthe elements and combinations particularly pointed out in the appendedclaims. It is to be understood that both the foregoing generaldescription and the following detailed description are exemplary andexplanatory only and are not restrictive of the invention, as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows Oxysense™ O₂ scavenging data for DCX-600 (hexa-functionalscavenger) and DC-300 (tetra-functional scavenger) containing plaques,as described in Example 2.

FIG. 2 shows Oxysense™ O₂ scavenging data for DCX-300-1 (di-functionalscavenger) and DC-300 (tetra-functional scavenger) containing plaques,as described in Example 3.

DETAILED DESCRIPTION

The present invention can be understood more readily by reference to thefollowing detailed description of the invention and the Examplesincluded therein.

Before the present compounds, compositions, articles, systems, devices,and/or methods are disclosed and described, it is to be understood thatthey are not limited to specific synthetic methods unless otherwisespecified, or to particular reagents unless otherwise specified, as suchmay, of course, vary. It is also to be understood that the terminologyused herein is for the purpose of describing particular aspects only andis not intended to be limiting. Although any methods and materialssimilar or equivalent to those described herein can be used in thepractice or testing of the present invention, example methods andmaterials are now described.

Disclosed are the components to be used to prepare the compositions ofthe invention as well as the compositions themselves to be used withinthe methods disclosed herein. These and other materials are disclosedherein, and it is understood that when combinations, subsets,interactions, groups, etc. of these materials are disclosed that whilespecific reference of each various individual and collectivecombinations and permutation of these compounds can not be explicitlydisclosed, each is specifically contemplated and described herein. Forexample, if a particular compound is disclosed and discussed and anumber of modifications that can be made to a number of moleculesincluding the compounds are discussed, specifically contemplated is eachand every combination and permutation of the compound and themodifications that are possible unless specifically indicated to thecontrary. Thus, if a class of molecules A, B, and C are disclosed aswell as a class of molecules D, E, and F and an example of a combinationmolecule, A-D is disclosed, then even if each is not individuallyrecited each is individually and collectively contemplated meaningcombinations, A-E, A-F, B-D, B-E, B-F, C-D, C-E, and C-F are considereddisclosed. Likewise, any subset or combination of these is alsodisclosed. Thus, for example, the sub-group of A-E, B-F, and C-E wouldbe considered disclosed. This concept applies to all aspects of thisapplication including steps in methods of making and using thecompositions of the invention. Thus, if there are a variety ofadditional steps that can be performed it is understood that each ofthese additional steps can be performed with any specific embodiment orcombination of embodiments of the methods of the invention.

While aspects of the present invention can be described and claimed in aparticular statutory class, such as the system statutory class, this isfor convenience only and one of skill in the art will understand thateach aspect of the present invention can be described and claimed in anystatutory class. Unless otherwise expressly stated, it is in no wayintended that any method or aspect set forth herein be construed asrequiring that its steps be performed in a specific order. Accordingly,where a method claim does not specifically state in the claims ordescriptions that the steps are to be limited to a specific order, it isno way intended that an order be inferred, in any respect. This holdsfor any possible non-express basis for interpretation, including mattersof logic with respect to arrangement of steps or operational flow, plainmeaning derived from grammatical organization or punctuation, or thenumber or type of aspects described in the specification.

Throughout this application, various publications are referenced. Thedisclosures of these publications in their entireties are herebyincorporated by reference into this application in order to more fullydescribe the state of the art to which this pertains. The referencesdisclosed are also individually and specifically incorporated byreference herein for the material contained in them that is discussed inthe sentence in which the reference is relied upon. Nothing herein is tobe construed as an admission that the present invention is not entitledto antedate such publication by virtue of prior invention. Further, thedates of publication provided herein may be different from the actualpublication dates, which can require independent confirmation.

As used in the specification and the appended claims, the singular forms“a,” “an” and “the” include plural referents unless the context clearlydictates otherwise. Thus, for example, reference to “a functionalgroup,” “an alkyl,” or “a residue” includes mixtures of two or more suchfunctional groups, alkyls, or residues, and the like.

Ranges can be expressed herein as from “about” one particular value,and/or to “about” another particular value. When such a range isexpressed, another aspect includes from the one particular value and/orto the other particular value. Similarly, when values are expressed asapproximations, by use of the antecedent “about,” it will be understoodthat the particular value forms another aspect. It will be furtherunderstood that the endpoints of each of the ranges are significant bothin relation to the other endpoint, and independently of the otherendpoint. It is also understood that there are a number of valuesdisclosed herein, and that each value is also herein disclosed as“about” that particular value in addition to the value itself. Forexample, if the value “10” is disclosed, then “about 10” is alsodisclosed. It is also understood that each unit between two particularunits are also disclosed. For example, if 10 and 15 are disclosed, then11, 12, 13, and 14 are also disclosed.

As used herein, the terms “optional” or “optionally” means that thesubsequently described event or circumstance may or may not occur, andthat the description includes instances where said event or circumstanceoccurs and instances where it does not.

As used herein, the term “substantially” means that the subsequentlydescribed event or circumstance completely occurs or that thesubsequently described event or circumstance generally, typically, orapproximately occurs. For example, when the specification discloses thatsubstantially all of an agent is released, a person skilled in therelevant art would readily understand that the agent need not becompletely released. Rather, this term conveys to a person skilled inthe relevant art that the agent need only be released to an extent thatan effective amount is no longer unreleased.

As used herein, the term “polymer” refers to a relatively high molecularweight organic compound, natural or synthetic, whose structure can berepresented by a repeated small unit, the monomer (e.g., polyethylene,rubber, cellulose). Synthetic polymers are typically formed by additionor condensation polymerization of monomers.

As used herein, the term “copolymer” refers to a polymer formed from twoor more different repeating units (monomer residues). By way of exampleand without limitation, a copolymer can be an alternating copolymer, arandom copolymer, a block copolymer, or a graft copolymer. It is alsocontemplated that, in certain aspects, various block segments of a blockcopolymer can themselves comprise copolymers.

As used herein, the term “oligomer” refers to a relatively low molecularweight polymer in which the number of repeating units is between two andten, for example, from two to eight, from two to six, or from two tofour. In one aspect, a collection of oligomers can have an averagenumber of repeating units of from about two to about ten, for example,from about two to about eight, from about two to about six, or fromabout two to about four.

As used herein, the term “star polymer” refers to a branched polymermolecule in which a single branch point gives rise to multiple linearchains or arms. The single branch point can be a single chemical moietyor can be a highly crosslinked section of polymer. In one aspect, a starpolymer can be generally spherical in shape. In a further aspect, a starpolymer can be particle shaped. If the arms are identical the starpolymer molecule is said to be regular. If adjacent arms are composed ofdifferent repeating subunits, the star polymer molecule is said to bevariegated.

As used herein, the term “molecular weight” (MW) refers to the mass ofone molecule of that substance, relative to the unified atomic mass unitu (equal to 1/12 the mass of one atom of carbon-12).

As used herein, the term “number average molecular weight” (M_(n))refers to the common, mean, average of the molecular weights of theindividual polymers. M_(n) can be determined by measuring the molecularweight of n polymer molecules, summing the weights, and dividing by n.M_(n) is calculated by:

${{\overset{\_}{M}}_{n} = \frac{\sum_{i}{N_{i}M_{i}}}{\sum_{i}N_{i}}},$

wherein N_(i) is the number of molecules of molecular weight M_(i). Thenumber average molecular weight of a polymer can be determined by gelpermeation chromatography, viscometry (Mark-Houwink equation), lightscattering, analytical ultracentrifugation, vapor pressure osmometry,end-group titration, and colligative properties.

As used herein, the term “weight average molecular weight” (M_(w))refers to an alternative measure of the molecular weight of a polymer.M_(w) is calculated by:

${{\overset{\_}{M}}_{w} = \frac{\sum_{i}{N_{i}M_{i}^{2}}}{\sum_{i}{N_{i}M_{i}}}},$wherein N_(i) is the number of molecules of molecular weight M_(i).Intuitively, if the weight average molecular weight is w, and a randommonomer is selected, then the polymer it belongs to will have a weightof w on average. The weight average molecular weight can be determinedby light scattering, small angle neutron scattering (SANS), X-rayscattering, and sedimentation velocity.

As used herein, the terms “polydispersity” and “polydispersity index”(PDI) refer to the ratio of the weight average to the number average(M_(w)/M_(n)).

As used herein, the term “compatibilizing agent” refers to a smallmolecule or polymer that has both polar and non-polar functional groups.For example, a fatty-acid ester has both polar and non-polar functionalgroups.

A weight percent (wt. %) of a component, unless specifically stated tothe contrary, is based on the total weight of the formulation orcomposition in which the component is included.

As used herein, nomenclature for compounds, including organic compounds,can be given using common names, IUPAC, IUBMB, or CAS recommendationsfor nomenclature. When one or more stereochemical features are present,Cahn-Ingold-Prelog rules for stereochemistry can be employed todesignate stereochemical priority, E/Z specification, and the like. Oneof skill in the art can readily ascertain the structure of a compound ifgiven a name, either by systemic reduction of the compound structureusing naming conventions, or by commercially available software, such asCHEMDRAW™ (Cambridgesoft Corporation, U.S.A.).

A residue of a chemical species, as used in the specification andconcluding claims, refers to the moiety that is the resulting product ofthe chemical species in a particular reaction scheme or subsequentformulation or chemical product, regardless of whether the moiety isactually obtained from the chemical species. Thus, an ethylene glycolresidue in a polyester refers to one or more —OCH₂CH₂O— units in thepolyester, regardless of whether ethylene glycol was used to prepare thepolyester. Similarly, a sebacic acid residue in a polyester refers toone or more —CO(CH₂)₈CO— moieties in the polyester, regardless ofwhether the residue is obtained by reacting sebacic acid or an esterthereof to obtain the polyester.

A very close synonym of the term “residue” is the term “radical,” whichas used in the specification and concluding claims, refers to afragment, group, or substructure of a molecule described herein,regardless of how the molecule is prepared. For example, a2,4-thiazolidinedione radical in a particular compound has the structure

regardless of whether thiazolidinedione is used to prepare the compound.In some embodiments the radical (for example an alkyl) can be furthermodified (i.e., substituted alkyl) by having bonded thereto one or more“substituent radicals.” The number of atoms in a given radical is notcritical to the present invention unless it is indicated to the contraryelsewhere herein.

In some aspects, a structure of a compound can be represented by aformula:

which is understood to be equivalent to a formula:

wherein n is typically an integer. That is, R^(n) is understood torepresent five independent substituents, R^(n(a)), R^(n(b)), R^(n(c)),R^(n(d)), R^(n(e)). By “independent substituents,” it is meant that eachR substituent can be independently defined. For example, if in oneinstance R^(n(a)) is halogen, then R^(n(b)) is not necessarily halogenin that instance.

As used herein, the term “substituted” is contemplated to include allpermissible substituents of organic compounds. In a broad aspect, thepermissible substituents include acyclic and cyclic, branched andunbranched, carbocyclic and heterocyclic, and aromatic and nonaromaticsubstituents of organic compounds. Illustrative substituents include,for example, those described below. The permissible substituents can beone or more and the same or different for appropriate organic compounds.For purposes of this disclosure, the heteroatoms, such as nitrogen, canhave hydrogen substituents and/or any permissible substituents oforganic compounds described herein which satisfy the valences of theheteroatoms. This disclosure is not intended to be limited in any mannerby the permissible substituents of organic compounds. Also, the terms“substitution” or “substituted with” include the implicit proviso thatsuch substitution is in accordance with permitted valence of thesubstituted atom and the substituent, and that the substitution resultsin a stable compound, e.g., a compound that does not spontaneouslyundergo transformation such as by rearrangement, cyclization,elimination, etc.

In defining various terms, “A¹,” “A²,” “A³,” and “A⁴” are used herein asgeneric symbols to represent various specific substituents. Thesesymbols can be any substituent, not limited to those disclosed herein,and when they are defined to be certain substituents in one instance,they can, in another instance, be defined as some other substituents.

The term “alkyl” as used herein is a branched or unbranched saturatedhydrocarbon group of from 1 to 24 carbon atoms, for example from 1 to 12carbons, from 1 to 8 carbons, from 1 to 6 carbons, or from 1 to 4carbons, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl,s-butyl, t-butyl, n-pentyl, isopentyl, s-pentyl, neopentyl, hexyl,heptyl, octyl, nonyl, decyl, dode cyl, tetradecyl, hexadecyl, eicosyl,tetracosyl, and the like. The alkyl group can be cyclic or acyclic. Thealkyl group can be branched or unbranched. The alkyl group can also besubstituted or unsubstituted. For example, the alkyl group can besubstituted with one or more groups including optionally substitutedalkyl, cycloalkyl, alkoxy, amino, ether, halide, hydroxy, nitro, silyl,sulfo-oxo, or thiol, as described herein. A “lower alkyl” group is analkyl group containing from one to six (e.g., from one to four) carbonatoms.

Throughout the specification “alkyl” is generally used to refer to bothunsubstituted alkyl groups and substituted alkyl groups; however,substituted alkyl groups are also specifically referred to herein byidentifying the specific substituent(s) on the alkyl group. For example,the term “halogenated alkyl” specifically refers to an alkyl group thatis substituted with one or more halide, e.g., fluorine, chlorine,bromine, or iodine. The term “alkoxyalkyl” specifically refers to analkyl group that is substituted with one or more alkoxy groups, asdescribed below. The term “alkylamino” specifically refers to an alkylgroup that is substituted with one or more amino groups, as describedbelow, and the like. When “alkyl” is used in one instance and a specificterm such as “alkylalcohol” is used in another, it is not meant to implythat the term “alkyl” does not also refer to specific terms such as“alkylalcohol” and the like.

This practice is also used for other groups described herein. That is,while a term such as “cycloalkyl” refers to both unsubstituted andsubstituted cycloalkyl moieties, the substituted moieties can, inaddition, be specifically identified herein; for example, a particularsubstituted cycloalkyl can be referred to as, e.g., an“alkylcycloalkyl.” Similarly, a substituted alkoxy can be specificallyreferred to as, e.g., a “halogenated alkoxy,” a particular substitutedalkenyl can be, e.g., an “alkenylalcohol,” and the like. Again, thepractice of using a general term, such as “cycloalkyl,” and a specificterm, such as “alkylcycloalkyl,” is not meant to imply that the generalterm does not also include the specific term.

The term “cycloalkyl” as used herein is a non-aromatic carbon-based ringcomposed of at least three carbon atoms. Examples of cycloalkyl groupsinclude, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, norbornyl, and the like. The term “heterocycloalkyl” is atype of cycloalkyl group as defined above, and is included within themeaning of the term “cycloalkyl,” where at least one of the carbon atomsof the ring is replaced with a heteroatom such as, but not limited to,nitrogen, oxygen, sulfur, or phosphorus. The cycloalkyl group andheterocycloalkyl group can be substituted or unsubstituted. Thecycloalkyl group and heterocycloalkyl group can be substituted with oneor more groups including optionally substituted alkyl, cycloalkyl,alkoxy, amino, ether, halide, hydroxy, nitro, silyl, sulfo-oxo, or thiolas described herein.

The terms “alkoxy” and “alkoxyl” as used herein to refer to an alkyl orcycloalkyl group bonded through an ether linkage; that is, an “alkoxy”group can be defined as —OA¹ where A¹ is alkyl or cycloalkyl as definedabove. “Alkoxy” also includes polymers of alkoxy groups as justdescribed; that is, an alkoxy can be a polyether such as —OA¹-OA² or—OA¹-(OA²)_(a)-OA³, where “a” is an integer of from 1 to 200 and A¹, A²,and A³ are alkyl and/or cycloalkyl groups.

The term “alkenyl” as used herein is a hydrocarbon group of from 2 to 24carbon atoms with a structural formula containing at least onecarbon-carbon double bond. Asymmetric structures such as (A¹A²)C═C(A³A⁴)are intended to include both the E and Z isomers. This can be presumedin structural formulae herein wherein an asymmetric alkene is present,or it can be explicitly indicated by the bond symbol C═C. The alkenylgroup can be substituted with one or more groups including optionallysubstituted alkyl, cycloalkyl, alkoxy, alkenyl, cycloalkenyl, alkynyl,cycloalkynyl, aryl, heteroaryl, aldehyde, amino, carboxylic acid, ester,ether, halide, hydroxy, ketone, azide, nitro, silyl, sulfo-oxo, orthiol, as described herein.

The term “cycloalkenyl” as used herein is a non-aromatic carbon-basedring composed of at least three carbon atoms and containing at least onecarbon-carbon double bound, i.e., C═C. Examples of cycloalkenyl groupsinclude, but are not limited to, cyclopropenyl, cyclobutenyl,cyclopentenyl, cyclopentadienyl, cyclohexenyl, cyclohexadienyl,norbornenyl, and the like. The term “heterocycloalkenyl” is a type ofcycloalkenyl group as defined above, and is included within the meaningof the term “cycloalkenyl,” where at least one of the carbon atoms ofthe ring is replaced with a heteroatom such as, but not limited to,nitrogen, oxygen, sulfur, or phosphorus. The cycloalkenyl group andheterocycloalkenyl group can be substituted or unsubstituted. Thecycloalkenyl group and heterocycloalkenyl group can be substituted withone or more groups including optionally substituted alkyl, cycloalkyl,alkoxy, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, heteroaryl,aldehyde, amino, carboxylic acid, ester, ether, halide, hydroxy, ketone,azide, nitro, silyl, sulfo-oxo, or thiol as described herein.

The term “alkynyl” as used herein is a hydrocarbon group of 2 to 24carbon atoms with a structural formula containing at least onecarbon-carbon triple bond. The alkynyl group can be unsubstituted orsubstituted with one or more groups including optionally substitutedalkyl, cycloalkyl, alkoxy, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl,aryl, heteroaryl, aldehyde, amino, carboxylic acid, ester, ether,halide, hydroxy, ketone, azide, nitro, silyl, sulfo-oxo, or thiol, asdescribed herein.

The term “cycloalkynyl” as used herein is a non-aromatic carbon-basedring composed of at least seven carbon atoms and containing at least onecarbon-carbon triple bond. Examples of cycloalkynyl groups include, butare not limited to, cycloheptynyl, cyclooctynyl, cyclononynyl, and thelike. The term “heterocycloalkynyl” is a type of cycloalkenyl group asdefined above, and is included within the meaning of the term“cycloalkynyl,” where at least one of the carbon atoms of the ring isreplaced with a heteroatom such as, but not limited to, nitrogen,oxygen, sulfur, or phosphorus. The cycloalkynyl group andheterocycloalkynyl group can be substituted or unsubstituted. Thecycloalkynyl group and heterocycloalkynyl group can be substituted withone or more groups including optionally substituted alkyl, cycloalkyl,alkoxy, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, heteroaryl,aldehyde, amino, carboxylic acid, ester, ether, halide, hydroxy, ketone,azide, nitro, silyl, sulfo-oxo, or thiol as described herein.

The term “aryl” as used herein is a group that contains any carbon-basedaromatic group including benzene, naphthalene, phenyl, biphenyl,phenoxybenzene, and the like. The term “aryl” also includes“heteroaryl,” which is defined as a group that contains an aromaticgroup that has at least one heteroatom incorporated within the ring ofthe aromatic group. Examples of heteroatoms include, but are not limitedto, nitrogen, oxygen, sulfur, and phosphorus. Likewise, the term“non-heteroaryl,” which is also included in the term “aryl,” defines agroup that contains an aromatic group that does not contain aheteroatom. The aryl group can be substituted or unsubstituted. The arylgroup can be substituted with one or more groups including optionallysubstituted alkyl, cycloalkyl, alkoxy, alkenyl, cycloalkenyl, alkynyl,cycloalkynyl, aryl, heteroaryl, aldehyde, amino, carboxylic acid, ester,ether, halide, hydroxy, ketone, azide, nitro, silyl, sulfo-oxo, or thiolas described herein. The term “biaryl” is a specific type of aryl groupand is included in the definition of “aryl.” Biaryl refers to two arylgroups that are bound together via a fused ring structure, as innaphthalene, or are attached via one or more carbon-carbon bonds, as inbiphenyl.

The term “aldehyde” as used herein is represented by the formula —C(O)H.Throughout this specification “C(O)” is a short hand notation for acarbonyl group, i.e., C═O.

The terms “amine” or “amino” as used herein are represented by theformula NA¹A²A³, where A¹, A², and A³ can be, independently, hydrogen oroptionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl,alkynyl, cycloalkynyl, aryl, or heteroaryl group as described herein.

The term “carboxylic acid” as used herein is represented by the formula—C(O)OH.

The term “ester” as used herein is represented by the formula —OC(O)A¹or —C(O)OA¹, where A¹ can be an optionally substituted alkyl,cycloalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, orheteroaryl group as described herein. The term “polyester” as usedherein is represented by the formula -(A¹O(O)C-A²-C(O)O)_(a)— or-(A¹O(O)C-A²-OC(O))_(a)—, where A¹ and A² can be, independently, anoptionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl,alkynyl, cycloalkynyl, aryl, or heteroaryl group described herein and“a” is an interger from 1 to 500. “Polyester” is as the term used todescribe a group that is produced by the reaction between a compoundhaving at least two carboxylic acid groups with a compound having atleast two hydroxyl groups.

The term “ether” as used herein is represented by the formula A¹OA²,where A¹ and A² can be, independently, an optionally substituted alkyl,cycloalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, orheteroaryl group described herein. The term “polyether” as used hereinis represented by the formula -(A¹O-A²O)_(a)—, where A¹ and A² can be,independently, an optionally substituted alkyl, cycloalkyl, alkenyl,cycloalkenyl, alkynyl, cycloalkynyl, aryl, or heteroaryl group describedherein and “a” is an integer of from 1 to 500. Examples of polyethergroups include polyethylene oxide, polypropylene oxide, and polybutyleneoxide.

The term “halide” as used herein refers to the halogens fluorine,chlorine, bromine, and iodine.

The term “heterocycle,” as used herein refers to single and multi-cyclicaromatic or non-aromatic ring systems in which at least one of the ringmembers is other than carbon. Heterocycle includes pyridinde,pyrimidine, furan, thiophene, pyrrole, isoxazole, isothiazole, pyrazole,oxazole, thiazole, imidazole, oxazole, including, 1,2,3-oxadiazole,1,2,5-oxadiazole and 1,3,4-oxadiazole, thiadiazole, including,1,2,3-thiadiazole, 1,2,5-thiadiazole, and 1,3,4-thiadiazole, triazole,including, 1,2,3-triazole, 1,3,4-triazole, tetrazole, including1,2,3,4-tetrazole and 1,2,4,5-tetrazole, pyridine, pyridazine,pyrimidine, pyrazine, triazine, including 1,2,4-triazine and1,3,5-triazine, tetrazine, including 1,2,4,5-tetrazine, pyrrolidine,piperidine, piperazine, morpholine, azetidine, tetrahydropyran,tetrahydrofuran, dioxane, and the like.

The term “hydroxyl” as used herein is represented by the formula —OH.

The term “ketone” as used herein is represented by the formula A¹C(O)A²,where A¹ and A² can be, independently, an optionally substituted alkyl,cycloalkyl, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, orheteroaryl group as described herein.

The term “azide” as used herein is represented by the formula —N₃.

The term “nitro” as used herein is represented by the formula —NO₂.

The term “nitrile” as used herein is represented by the formula —CN.

The term “thiol” as used herein is represented by the formula —SH.

Certain instances of the above defined terms may occur more than once inthe structural formulae, and upon such occurrence each term shall bedefined independently of the other.

As used herein, the term “effective amount” refers to an amount that issufficient to achieve the desired result or to have an effect on anundesired condition. For example, a “visually effective amount” refersto an amount that is sufficient to achieve the desired result (i.e.,impart color to a composition or an article), but is generallyinsufficient to cause adverse side affects (e.g., warping of a polymericarticle).

The term “leaving group” refers to an atom (or a group of atoms) withelectron withdrawing ability that can be displaced as a stable species,taking with it the bonding electrons. Examples of suitable leavinggroups include sulfonate esters, including triflate, mesylate, tosylate,brosylate, and halides.

Compounds described herein can contain one or more double bonds and,thus, potentially give rise to cis/trans (E/Z) isomers, as well as otherconformational isomers. Unless stated to the contrary, the inventionincludes all such possible isomers, as well as mixtures of such isomers.

Unless stated to the contrary, a formula with chemical bonds shown onlyas solid lines and not as wedges or dashed lines contemplates eachpossible isomer, e.g., each enantiomer and diastereomer, and a mixtureof isomers, such as a racemic or scalemic mixture. Compounds describedherein can contain one or more asymmetric centers and, thus, potentiallygive rise to diastereomers and optical isomers. Unless stated to thecontrary, the present invention includes all such possible diastereomersas well as their racemic mixtures, their substantially pure resolvedenantiomers, all possible geometric isomers, and pharmaceuticallyacceptable salts thereof. Mixtures of stereoisomers, as well as isolatedspecific stereoisomers, are also included. During the course of thesynthetic procedures used to prepare such compounds, or in usingracemization or epimerization procedures known to those skilled in theart, the products of such procedures can be a mixture of stereoisomers.

The disclosed compounds are N-allylic amide compounds or N-benzylicamide compounds. The amide compound is useful as an oxygen scavenger.The oxygen scavenging ability of the amide compound can be enhanced, invarious aspects, by the presence of a transition metal.

The disclosed N-allylic or N-benzylic amide compounds have the generalstructure shown below:

wherein each - - - independently denotes an optional covalent bond.

The N-allylic or N-benzylic amide compound can be further substitutedand more than one amide functionality can be present in a compound. Inone aspect, an N-allylic or N-benzylic amide compound can be polymeric.In a further aspect, an N-allylic or N-benzylic amide compound can benonpolymeric.

In one aspect, the amide compound has a structure of Formula I or II:

wherein the symbol - - - when used in conjunction with a bond linerepresents a single or a double bond; wherein n is 3, 4, 5, or 6;wherein m is an integer from 0 to 6-n; wherein each X is independentlyselected from the group consisting of O, S, and NH; wherein each Y, eachA, and each B are independently selected from the group consisting of N,CR¹, and CR²; wherein D, E, and F are independently selected from thegroup consisting of CH, N, O, and S; and wherein each R¹ and each R² isindependently selected from the group consisting of H, alkyl, aryl,electron withdrawing groups, electron releasing groups, and a transitionmetal.

In one aspect, the compound of formula I or II can be represented by thefollowing formula:

In a further aspect, the compound has a structure of Formula III orFormula IV:

wherein the symbol - - - when used in conjunction with a bond linerepresents a single or a double bond; wherein each n is independently1-5; wherein m is an integer from 0 to 5-n;wherein each X is independently selected from the group consisting of O,S, and NH;wherein each Y, each A, and each B are independently selected from thegroup consisting of N, CR¹, and CR²; wherein D, E, and F areindependently selected from the group consisting of CH, N, O, and S;wherein each R¹ and each R² is independently selected from the groupconsisting of H, alkyl, aryl, electron withdrawing groups, electronreleasing groups, and a transition metal; and wherein L is a divalentlinking group selected from C2-C12 aliphatic or cyclic ether, C2-C12aliphatic or cyclic amide, C6 to C12 aromatic amide, C2-C12 aliphatic orcyclic amine, C6-C12 aromatic amine, C2-C12 aliphatic or cyclic esterand C6 to C12 aromatic ester.

In a further aspect, the compound has a structure of Formula V orFormula VI:

wherein the symbol - - - when used in conjunction with a bond linerepresents a single or a double bond; wherein each n is independently0-5; wherein m is an integer from 0 to 5-n; wherein each X isindependently selected from the group consisting of O, S, and NH;wherein each Y, each A, and each B are independently selected from thegroup consisting of N, CR¹, and CR²; wherein D, E, and F areindependently selected from the group consisting of CH, N, O, and S;wherein each R¹ and each R² is independently selected from the groupconsisting of H, alkyl, aryl, electron withdrawing groups, electronreleasing groups, and a transition metal; and wherein L is a divalentlinking group selected from C2-C12 aliphatic or cyclic ether, C2-C12aliphatic or cyclic amide, C6 to C12 aromatic amide, C2-C12 aliphatic orcyclic amine, C6-C12 aromatic amine, C2-C12 aliphatic or cyclic esterand C6 to C12 aromatic ester.

Generally, linking group L is a divalent organic residue. Suitablelinking groups L include divalent aliphatic chains, divalent aliphaticor cyclic ethers, divalent aliphatic or cyclic amides, divalent aromaticamide, divalent aliphatic or cyclic amines, divalent aromatic amines,divalent aliphatic or cyclic esters and divalent aromatic esters, suchas those exemplified in Table 1 below. As used in the table below, theterm “tether compound” refers to a difunctional organic compound capableof reactions with ring substitutents of disclosed moieties to formcovalent bonds, thereby chemically connecting the ring substitutents viaa divalent organic residue of the tether compound, refered to as alinking group, L. Examples of tether compounds include dielectrophiliccompounds (e.g., diacyl halides, cyclic anhydrides, and bis-alkylhalides) for linking nucleophilic ring substituents (e.g., hydroxides,thiols, and amines). Further examples of tether compounds includedinucleophilic compounds (e.g., bis-hydroxides, bis-thiols, andbis-amines) for linking electrophilic ring substituents (e.g., acylhalides and alkyl halides). Selected examples are illustratedstructurally in Table 1.

TABLE 1 Ring L Substituent Tether Compound

In Table 1, R is an optionally substituted divalent organic residue; forexample, R can be selected from optionally substituted alkyl or alkenylor alkynyl, optionally substituted heteroalkyl or heteroalkenyl orheteroalkynyl, optionally substituted cycloalkyl or cycloalkenyl orcycloalkynyl, optionally substituted heterocycloalkyl orheterocycloalkenyl or heterocycloalkynyl, optionally substituted aryl,and optionally substituted heteroaryl. In further aspects, R can belinear, cyclic, or branched. Typically, R has from 1 to 48 carbons, from1 to 24 carbons, from 1 to 12 carbons, from 1 to 8 carbons, from 1 to 6carbon, or from 1 to 4 carbons.

In further aspects, R′ is an optionally substituted organic residue.Typically, R′ has from 1 to 12 carbons, from 1 to 8 carbons, from 1 to 6carbon, or from 1 to 4 carbons. For example, R′ can be methyl, ethyl,propyl, butyl, pentyl, or hexyl.

It is also contemplated that the functional groups selected for use infabricating L can be used in combinations other than those shown in theTable. For example, in a further aspect, L can be:

Linking groups L can be readily prepared by methods known to those ofskill in the art of organic synthesis.

The alkyl group of the compound of Formulae (I-VI) can be a branched orunbranched saturated hydrocarbon group of 1 to 24 carbon atoms, e.g. 1to 18 carbons atoms, 1 to 14 carbon atoms, 1 to 12 carbon atoms, 1 to 10carbon atoms, 1 to 8, 1 to 6 carbon atoms, or 1 to 4 carbon atoms, suchas methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl,pentyl, hexyl, heptyl, octyl, decyl, tetradecyl, hexadecyl, eicosyl,tetracosyl and the like. The alkyl group can be substituted orunsubstituted. The alkyl group can be substituted with one or moregroups including, but not limited to, alkyl, halogenated alkyl, alkoxy,alkenyl, alkynyl, aryl, heteroaryl, aldehyde, amino, carboxylic acid,ester, halide, hydroxamate, hydroxy, ketone, nitro, silyl, sulfo-oxo,sulfonyl, sulfone, sulfoxide, or thiol, as described below. The alkylgroup can be halogenated, which includes an alkyl group that issubstituted with one or more halide, e.g., fluorine, chlorine, bromine,or iodine. The alkyl group can also be a lower alkyl group, which is analkyl group containing from one to six (e.g., from one to four) carbonatoms.

The aryl group of the compound of Formulae (I-VI) can be anycarbon-based aromatic group including but not limited to, benzene,naphthalene, phenyl, biphenyl, etc. The aryl group can also beheteroaryl, which is defined as an aromatic group that has at least oneheteroatom incorporated within the ring of the aromatic group. Examplesof heteroatoms include, but are not limited to, nitrogen, oxygen,sulfur, and phosphorus. The aryl group can be substituted orunsubstituted. The aryl group can be substituted with one or more groupsincluding, but not limited to, alkyl, halogenated alkyl, alkoxy,alkenyl, alkynyl, aryl, heteroaryl, aldehyde, amino, carboxylic acid,ester, halide, hydroxamate, hydroxy, ketone, nitro, silyl, sulfo-oxo,sulfonyl, sulfone, sulfoxide, or thiol as described herein. A biarylgroup is a specific type of aryl group and is included in the definitionof aryl. Biaryl refers to two aryl groups that are bound together via afused ring structure, as in naphthalene, or are attached via one or morecarbon-carbon bonds, as in biphenyl.

Suitable electron withdrawing groups and electron releasing groups aregenerally known in the art. Preferred electron withdrawing groupsinclude nitro, carboxylic acid, esters, for example loweralkyl esters,and cyano. Preferred electron releasing groups include branched andstraight chain alkyl groups, for example, methyl, ethyl, propyl,isopropyl, butyl, isobutyl, and tert-butyl. Other preferred electronreleasing groups include alkoxy, for example methoxy and ethoxy. Otherpreferred electron releasing groups include thioalkyl. Still otherpreferred electron releasing groups include amines, for example —NH₂,and NH(loweralkyl), and N(loweralkyl)₂.

Oxygen scavenging amide compounds are disclosed in U.S. PatentApplication Publication No. 20080277622, Deshpande et al. “OxygenScavenging Molecules, Articles Containing Same, And Methods of TheirUse,” which is incorporated herein by this reference for its teaching ofamide compounds, their preparation, and their use as oxygen scavengingmaterials.

One version of Compound I can be prepared by reacting one mole of1,3,5-trimethylaminobenzene with three moles of 1-isoindolinone (CAS#87-41-2) in a continuous stirred tank reactor (CSTR) using a solventsuch as xylene under N2 pressure and at temperatures exceeding 200° C.After distilling off water as a byproduct of the reaction, the reactionproduct is isolated and purified using successive solvent washes.

One version of Compound II can be prepared by reacting one mole of1,3,5-trimethylaminobenzene with three moles of phthalic anhydride undersimilar reaction and purification conditions described above.

One version of Compound V with an ester linking group L can be preparedby reaction of 2 moles of meta-xylene bis (5-carboxyisoindolin-1-one)with one mole of a diol in an acidic environment to yield a structuresimilar to that described in Compound V. It is possible to use aliphaticdiols such as ethylene glycol or cyclic diols such as1,4-cyclohexanediol or aromatic diols such as benzene-1,4-diol aslinking groups

One version of Compound V with an amide linking group L can be preparedby reaction of 2 moles of meta-xylene bis (5-carboxyisoindolin-1-one)with one more of a diamine to yield a structure similar to thatdescribed in Compound V. It is possible to use aliphatic diamines suchas ethylene diamine or cyclic diamines such as 1,4-cyclohexanediamine oraromatic diamines such as 1,4-phenylenediamine

One version of Compound V with an ether linking group can be prepared bythe reaction of 2 moles of meta-xylene bis(5-hydroxylisoindolin-1-one)with one mole of 1,2-dichloroethane to yield a structure similar to thatdescribed by compound V. Alternatively, one can use 2 moles ofmeta-xylene bis (5-chloroisoindolin-1-one) to react with itself inpresence of sodium benzoate (or any sodium salt of organic acid) andheat to give an ether linking group, similar to that described inCompound V. It is possible to use aliphatic dichloro compounds or cyclicdichloro compounds or aromatic dichloro compounds to obtain a range ofether based linking groups.

One version of Compound V with amine based linking group can be preparedby reaction of one mole of meta-xylene bis (5-chloroisoindolin-1-one)with one mole of meta-xylene bis (5-aminoisoindolin-1-one) in an basicmedium with heat to yield Compound V with an amine based linking group.Another version of Compound V with an amine based linking group can beprepared by reaction of 2 moles of meta-xylene bis(5-chloroisoindolin-1-one) with one mole of ethylene diamine in a basicmedium to yield a amine linked Compound V. It is possible to usealiphatic diamino compounds or cyclic diamino compounds or aromaticdiamino compounds to obtain a range of amine based linking groups.

The amide compound can in certain aspects be complexed to a transitionmetal. For example, the amide compound can be complexed to thetransition metal through one or more aryl groups, for example throughpi-cloud complexation. The amide compound can also be polymerized viacomplexation to the transition metal.

Also disclosed are polymer compositions. Generally, the disclosedpolymer composition comprises a base polymer; an amide compound ofFormula I-VI present in an amount of from about 0.10 to about 10 weightpercent of the composition; and optionally, a transition metal in apositive oxidation state, the metal present in an amount of from about10 ppm to about 400 ppm.

Generally, the amide compound is present in the composition in an amountof from 0.1 to about 10 weight percent. In one aspect, the amidecompound is present in the composition in an amount of from 1 to about10 weight percent. In a further aspect, the amide compound is present inthe composition in an amount of from 1 to about 5 weight percent. In afurther aspect, the amide compound is present in the composition in anamount of from 1 to about 3 weight percent.

A variety of different polymers can be used as the base polymer. Thedisclosed compositions enable oxygen scavenging, and thus the basepolymer generally includes those polymers that can be subject tooxidation. For example, polymers that exhibit at least some oxygenpermeability are useful with the disclosed compositions, at leastinasmuch as the disclosed compositions can reduce the oxidative damageto the polymer.

The base polymer can be a polymer commonly used in packaging materialsincluding polyethylene, such as low density polyethylene, very lowdensity polyethylene, ultra-low density polyethylene, high densitypolyethylene, and linear low density polyethylene; polyesters such as(PET), (PEN) and their copolymers such as PET/IP; polyvinyl chloride(PVC); polyvinylidene chloride (PVDC); and ethylene copolymers such asethylene/vinyl acetate copolymer, ethylene/alkyl (meth)acrylatecopolymers, ethylene/(meth)acrylic acid copolymers, and ionomers. Blendsof different base polymers also can be used.

In a further aspect, the base polymer can include one or more polymersapproved by the U.S. Food and Drug Admistration (FDA). Examples includepolyethylene terephthalate, polypropylene, and polyethylene.

In a further aspect, the base polymer comprises a polyester polymer orcopolymer. Preferred polyesters include polymers of phthalic acids, suchas polyethylene terephthalate (PET), or a copolymer thereof. PET, forexample, can be made from terephthalic acid and ethylene glycol. PET canalso be made using dimethyl terephthalate and ethylene glycol. Preferredcopolymers of phthalic acids include copolymers of a phthalic acid andone or more hydroxylated organic compounds. Examples of suitablehydroxylated organic compounds include 1, 4-cyclohexandedimethanol,1,2-propanediol, 1,4-butanediol, 2,2-dimethyl-1, 3-propanediol,2-methyl-1,3-propanediol (2MPDO), 1,6-hexanediol, 1,2-cyclohexanediol,1,4-cyclohexanediol, 1,2-cyclohexanedimethanol,1,3-cyclohexanedimethanol, and diols containing one or more oxygen atomsin the chain, e.g., diethylene glycol, triethylene glycol, dipropyleneglycol, tripropylene glycol, or mixtures of these, and the like.

In a still further aspect, the base polymer includes a polyethyleneterephthalate homopolymer and copolymer modified with one or morepolycarboxylic acid modifiers in a cumulative amount of less than about15 mole %, or about 10 mole % or less, or about 8 mole % or less, or oneor more hydroxyl compound modifiers in an amount of less than about 60mol %, or less than about 50 mole %, or less than about 40 mole %, orless than about 15 mole %, or about 10 mole % or less, or about 8 mole %or less and polyethylene naphthalate homopolymers and copolymersmodified with a cumulative amount of less than about 15 mole %, or about10 mole % or less, or about 8 mole % or less, of one or morepolycarboxylic acid modifiers or modified with less than about 60 mol %,or less than about 50 mole %, or less than about 40 mole %, or less thanabout 15 mole %, or about 10 mole % or less, or about 8 mole % or lessof one or more hydroxyl compound modifiers, and blends thereof. In someaspects, the base polymer comprises at least 90 mole %, 92 mole %, or 94mole % ethylene terephthalate repeat units based on the moles of allrepeat units in the polyester polymers.

Polyesters such as PET can be prepared by polymerization proceduresknown in the art sufficient to effect esterification andpolycondensation. Polyester melt phase manufacturing processes includedirect condensation of a dicarboxylic acid with a diol, optionally inthe presence of one or more esterification catalysts, in theesterification zone, followed by polycondensation in the prepolymer andfinishing zones in the presence of a polycondensation catalyst; or esterexchange usually in the presence of a transesterification catalyst inthe ester exchange zone, followed by prepolymerization andpolymerization in the presence of a polycondensation catalyst.

As briefly discussed above, the composition can optionally comprise atransition metal in a positive oxidation state. The transition metalenhances the oxygen scavenging properties of the amide compound. Amountsof transition metal in the composition can be greater than zero and canbe up to 5000 ppm. Generally, the transition metal will be present in anamount of from about 10 ppm to about 400 ppm. In one aspect, about 200ppm of the transition metal is present. In a further aspect, about 250ppm of the transition metal is present. In wall applications (as opposedto master batch applications where more transition metal is used), itcan be preferred to keep the level of metal below 300, more preferably250 ppm. In a further aspect, the transition metal is present from 30 to150 ppm. In a further aspect, about 50 ppm of the transition metal ispresent. In a further aspect, about 100 ppm of the transition metal ispresent. In a further aspect, about 150 ppm of the transition metal ispresent.

In one aspect, the transition metal can be a transition metal from thefirst, second, or third transition series of the Periodic Table. Themetal can be Rh, Ru, or one of the elements in the series of Sc to Zn(e.g., Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn). In one aspect, thetransition metal is cobalt. Cobalt can be used in +2 or +3 oxidationstates. In some aspects, it is preferred to use cobalt in the +2oxidation state. In a further aspect, the transition metal is rhodium.For example, rhodium in the +2 oxidation state can be used. Thetransition metal can also be a positive oxidation form of zinc.

The transition metal can be present as a salt. The cation of the saltcan be the transition metal in a positive oxidation state. A variety ofanions can stabilize the positively charged transition metal. Suitableanions for the salts include, but are not limited to, chloride, acetate,oleate, stearate, palmitate, 2-ethylhexanoate, carboxylates, such asneodecanoates, octanoates, acetates, lactates, naphthalates, malates,stearates, acetylacetonates, linoleates, oleates, palmitates,2-ethylhexanoates, or ethylene glycolates; or as their oxides, borates,carbonates, dioxides, hydroxides, nitrates, phosphates, sulfates, orsilicates, among others. Representative transition metal salts includecobalt (II) 2-ethylhexanoate, cobalt oleate, and cobalt (II)neodecanoate. The transition metal salt also can be an ionomer, in whichcase a polymeric counter ion can be present.

In one aspect, the composition can comprise a colorant in a visuallyeffective amount. A visually effective amount refers to an amount ofcolorant that results in the composition or an article made therefromappear colored to the naked eye. A composition comprising a visuallyeffective amount of colorant can refer to a composition having at least0.01% by weight colorant. In a further aspect, the composition cancomprise at least 0.25% by weight colorant. In a still further aspect,the composition can comprise at least 0.5% by weight colorant. Thecompositions can also comprise up to or even exceed about 3% by weightcolorant.

A visually effective amount can be determined, for example, byperforming a spectrophotometric scan of the composition or article usinga wavelength range from 400 to 700 nm (visible region). Specific colorscan be characterized according to their spectral pattern. Every coloralso has its own characteristic L (lightness gradation), a (red togreen) and b (yellow to blue) numbers, which can be used to characterizethe compositions and articles.

The colorant can be a variety of pigments and dyes, many of which arecommercially available. Examples of colorants include without limitationCOLORMATRIX Dark Amber, product code: 189-10034-6, COLORMATRIX Dead LeafGreen, product codes: 284-2801-3 and 84-2801-1, AMERICHEM amber, productcode: 59108-CD1, Champaigne green, and COLORMATRIX amber, product code:189-10100-1.

The composition can include other components such as fillers,crystallization aids, impact modifiers, surface lubricants, denestingagents, stabilizers, ultraviolet light absorbing agents, metaldeactivators, nucleating agents such as polyethylene and polypropylene,phosphate stabilizers and dyestuffs. Typically, the total quantity ofsuch components will be less than about 10% by weight of thecomposition. In some embodiments, the amount of these optionalcomponents is less than about 5% by weight of the composition.

The composition can comprise a reheat additive. Reheat additives arecommonly used in the manufacture of polyester polymer compositions usedto make stretch blow molded bottles because the preforms made from thecomposition must be reheated prior to entering the mold for stretchblowing into a bottle. Any conventional reheat additive can be used,such as various forms of black particles, e.g., carbon black, activatedcarbon, black iron oxide, glassy carbon, silicon carbide, gray particlessuch as antimony, and other reheat additives such as silicas, red ironoxide, and the like.

The composition can also comprise an impact modifier. Examples oftypical impact modifiers useful in the composition includeethylene/acrylate/glycidyl terpolymers and ethylene/acrylate copolymersin which the acrylate is a methyl or ethyl acrylate or methyl or ethylmethacrylate or the corresponding butyl acrylates, styrene based blockcopolymers, and various acrylic core/shell type impact modifiers. Theimpact modifiers can be used in conventional amounts from about 0.1 toabout 25 weight percent of the overall composition and, in some aspects,in amounts from about 0.1 to about 10 weight percent of the composition.

In many applications, not only are the packaging contents sensitive tothe ingress of oxygen, but the contents may also be affected by UVlight. Fruit juices and pharmaceuticals are two examples of suchcontents. Accordingly, in some aspects, it is desirable to incorporateinto the composition a UV absorbing compound in an amount effective toprotect the packaged contents.

The composition or an article made therefrom can have an OxygenTransmission Rate (OTR) of less than about 0.1 (units of cc/pkg/day or1-5 cc-mm/m²-day-atm) under standard conditions. In a further aspect,the OTR can be less than 0.03, less than 0.01, less than 0.005, or lessthan 0.001. The OTR is a measure of how well the amide compoundfunctions at scavenging oxygen that permeates the composition orarticle.

When OTR is expressed for a given composition or article, the units“cc/package/day” (“cc/pkg/day”) are typically employed. The term packagerefers to a barrier between an atmosphere of relatively lower oxygencontent and an atomosphere of relatively higher oxygen content. Typicalbarriers (e.g., packages) include bottles, thermoformed containers, andfilms (e.g., shrink wrap).

Oxygen Transmission Rate (oxygen permeation) can be measured, forexample, as described in U.S. Pat. No. 5,021,515. A material of area Acan be exposed to a partial pressure p of oxygen on the one side and toan essentially zero partial pressure of oxygen on the other side. Thequantity of oxygen emerging on the latter side is measured and expressedas a volume rate dV/dt, the volume being converted to some standardcondition of temperature and pressure. After a certain time of exposure(usually a period of a few days) dV/dt is generally found to stabilize,and a P_(w) value can be calculated from equation below:dV/dt=P _(W) Ap  (1)

P_(W) refers to the permeance of the wall. (Analogy with magneticpermeance and electrical conductance would suggest that P_(W) should bedescribed as “permeance per unit area”, but we are following thenomenclature in Encyclopaedia of Polymer Science and Technology, Vol. 2,Wiley Interscience, 1985, page 178.) The standard conditions forexpressing dV/dt are 0° C. and 1 atm (1 atm=101 325 Nm⁻²). If thethickness of the area of wall is substantially constant over the area Awith value T and the wall is uniform through the thickness (i.e., thewall is not a laminated or coated one) then the permeability of thematerial in the direction normal to the wall is calculated from theequation below.dV/dt=P _(M) Ap/T  (2)

For non-scavenging materials, P_(W) and P_(M) are to a reasonableapproximation independent oft and p, and P_(M) of T although they areoften appreciably dependent on other conditions of the measurement suchas the humidity of the atmosphere on the oxygen-rich side and thetemperature of the measurement.

For oxygen-scavenging walls, P_(W) and P_(M) are functions oft becausethe concentrations and activity of scavenger vary with time(particularly as the scavenger is consumed). This typically does notprevent measurement of P_(W) and P_(M) reasonably accurately as afunction of time, because the changes in dV/dt are relatively gradualonce the normal initial equilibration period of a few days is over.After a few days' exposure to the measurement conditions, however, anon-scavenging material typically achieves a steady state in which dV/dtis equal to the rate of oxygen ingress to the wall, while a scavengingmaterial achieves an (almost) steady state in which dV/dt isconsiderably less than the rate of oxygen ingress to the material. Thisbeing the case, it is likely that P_(W) calculated from (1) is afunction of p as well as oft and that P_(M) in (2) is a function of pand T as well as of t. P_(W) and P_(M) for scavenging materials are,strictly speaking, not true permeances and permeabilities at all (sincepermeation and scavenging are occurring simultaneously) but, rather,apparent ones.

Values of P_(W) and P_(M) (except where stated otherwise) are to beunderstood to refer to conditions in which p=0.21 atm, the relativehumidity on the oxygen-rich side of the wall is 50%, the temperature is23° C. and (in the case of P_(M) values) the thickness of the materialof about 0.45 mm. Conditions close to the first three of these, atleast, are conventional in the packaging industry.

For example, OTR can be measured for bottles, for example, bycontrolling the atmosphere on both sides of a sample of bottles andmeasuring the rate of oxygen permeation over time. Typically, thebottles are mounted on a plate such that there are two ports for gasinlet and outlet. The interior of the bottles is separated from theexterior by an air tight seal. After sealing, the interior of the bottleis flushed with N₂ gas (or N₂+H₂ mixture) to remove any oxygen presentbefore mounting on plate. The bottle is then placed in a controlledenvironmental chamber (maintained at 23° C. and 50% RH) such that theexterior of the bottle is at standard atmosphere with ˜21% oxygen. Theinterior of the bottle is continuously flushed with N₂ (or N₂+H₂) at aknown gas flow rate. The outlet of the flushed gases contains oxygenpermeating through the bottle wall. This flushed gas from the bottleinterior is passed over a sensor that is calibrated to measure oxygencontent of the flushed gas. Such measurements of oxygen content are madecontinously over time until a steady state is reached. This steady statevalue is typically reported as Oxygen Transmission Rate (OTR) for thatbottle in the units of cc/package/day. A preferred OTR for PET bottlesis less than 0.1 cc/package/day; more preferred is less than 0.01cc/package/day; most preferred for PET bottles is less than 0.001cc/package/day over the shelf life of the packaged product.

In one aspect, a disclosed composition has an OTR of less than that ofan otherwise identical composition in the absence of the amide compoundand the transition metal. In further aspects, a disclosed compositionhas an OTR of less than about 75%, less than about 50%, less than about25%, less than about 20%, less than about 10%, less than about 5%, orless than about 1% of an otherwise identical composition in the absenceof the amide compound and the transition metal.

Various methods exist for making the composition. In one aspect, thecomposition can be made by mixing the base polymer with the amidecompound and optionally the transition metal. In some aspects, some orpart of the transition metal may already be present in the base polymerprior to mixing, for example if the transition metal is used as acatalyst for making the base polymer. In some aspects, the base polymer,the oxidizable organic component and the transition metal are mixed bytumbling in a hopper. Other optional ingredients can be added duringthis mixing process or added to the mixture after the aforementionedmixing or to an individual component prior to the aforementioned mixingstep.

When melt processing is desired for the composition, the composition canalso be made by adding each ingredient separately and mixing theingredients just prior to melt processing the composition to form anarticle. In some embodiments, the mixing can be just prior to the meltprocess zone. In other embodiments, one or more ingredients can bepremixed in a separate step prior to bringing all of the ingredientstogether.

In some aspects, the transition metal can be added neat or in a carrier(such as a liquid or wax) to an extruder or other device for making thearticle, or the metal can be present in a concentrate or carrier withthe amide compound, in a concentrate or carrier with the base polymer,or in a concentrate or carrier with a base polymer/amide compound blend.It is desirable that the addition of the transition metal does notsubstantially increase the intrinsic viscosity of the melt in the meltprocessing zone. Thus, transition metal or metals can be added in two ormore stages, such as once during the melt phase for the production ofthe base polymer and again once more to the melting zone for making thearticle.

The melt blend of base polymer, amide compound, and transition metalcatalyst can also be prepared by adding the components at the throat ofan injection molding machine that: (i) produces a preform that can bestretch blow molded into the shape of the container, (ii) produces afilm that can be oriented into a packaging film, (iii) produces a sheetthat can be thermoformed into a food tray, or (iv) produces an injectionmolded container. The mixing section of the extruder should be of adesign to produce a homogeneous blend. Such process steps work well forforming carbonated soft drink, water or beer bottles, packaging filmsand thermoformed trays. The present invention can be employed in any ofthe conventional known processes for producing a polymeric container,film, tray, or other article that would benefit from oxygen scavenging.

Various articles can be prepared from the disclosed compositions. Thus,the articles prepared from the compositions will also have thecomposition present in the article. Suitable articles include vesselsand films, such as flexible sheet films, flexible bags, pouches,semi-rigid and rigid containers such as bottles (e.g. PET bottles) ormetal cans, or combinations thereof. Typical flexible films and bagsinclude those used to package various food items and can be made up ofone or a multiplicity of layers to form the overall film or bag-likepackaging material. The composition of the present invention can be usedin one, some or all of the layers of such packaging material.

Specific articles include preforms, containers and films for packagingof food, beverages, cosmetics, pharmaceuticals, and personal careproducts where a high oxygen barrier is needed. Examples of beveragecontainers are bottles for holding water and carbonated soft drinks, andthe invention is particularly useful in bottle applications containingjuices, sport drinks, beer or any other beverage where oxygendetrimentally affects the flavor, fragrance, performance (e.g., vitamindegradation), or color of the drink. The compositions are alsoparticularly useful as a sheet for thermoforming into rigid packages andfilms for flexible structures. Rigid packages include food trays andlids. Examples of food tray applications include dual ovenable foodtrays, or cold storage food trays, both in the base container and in thelidding (whether a thermoformed lid or a film), where the freshness ofthe food contents can decay with the ingress of oxygen. The compositionscan also be used in the manufacture of cosmetic containers andcontainers for pharmaceuticals or medical devices.

Other suitable articles include rigid or semi-rigid articles includingplastic, such as those utilized for juices, soft drinks, as well asthermoformed trays or cup normally having thickness in the range of from100 to 1000 micrometers. The walls of such articles can comprise singleor multiple layers of materials. The article can also take the form of abottle or can, or a crown, cap, crown or cap liner, plastisol or gasket.The composition of the present invention can be used as an integrallayer or portion of, or as an external or internal coating or liner of,the formed semi-rigid or rigid packaging article. As a liner, thecomposition can be extruded as a film along with the rigid articleitself, e.g., by coextrusion, extrusion coating, or an extrusionlamination process, so as to form the liner in situ during articleproduction; or alternatively can be adhered by heat and/or pressure, byadhesive, or by any other suitable method.

When the compositions are used in a wall or as a layer of a wall, thepermeability of the composition for oxygen is advantageously not morethan about 3.0, or about 1.7, or about 0.7, or about 0.2, or about 0.03cm³-mm/(m²-atm-day). In some aspects, the permeability of thecomposition is not more than about three-quarters of that in the absenceof the amide compound. In some aspects, the permeability is not morethan about one half, one-tenth in certain embodiments, one twenty-fifthin other embodiments, and not more than one-hundredth of that in theabsence of the amide compound.

Although it can be preferable from the standpoint of packagingconvenience and/or scavenging effectiveness to employ the presentinvention as an integral or discrete part of the packaging wall, theinvention can also be used as a non-integral component of a packagingarticle such as, for example, a bottle cap liner, adhesive ornon-adhesive sheet insert, sealant, sachet, fibrous mat insert or thelike.

Besides articles applicable for packaging food and beverage, articlesfor packaging other oxygen-sensitive products can also benefit from thepresent invention. Such products would include pharmaceuticals, oxygensensitive medical products, corrodible metals or products, electronicdevices and the like.

In a further aspect, the composition can be used as a master batch forblending with a polymer or a polymer containing component. In suchcompositions, the concentration of the amide compound and the transitionmetal will be high enough to allow for the final blended product to havesuitable amounts of these components. The master batch can also containan amount of the base polymer with which the master batch is blended.

Oxygen permeability of an article can be maintained for a longer periodof time by storing the article in a sealed container or under an inertatmosphere such as nitrogen prior to use with oxygen sensitivematerials.

The articles can be made by various methods known in the art. Generally,the articles are prepared by melt processing methods (i.e., a melt ofthe composition). Such processes generally include injection molding,stretch blow molding, extrusion, thermoforming, extrusion blow molding,and (specifically for multilayer structures) coextrusion and laminationusing adhesive tie layers. Orientation, e.g., by stretch blow molding,of the polymer can be used with phthalate polyesters because of theknown mechanical advantages that result.

The melt processing zone for making the article can be operated undercustomary conditions effective for making the intended articles, such aspreforms, bottles, trays, and other articles mentioned above. In oneaspect, such conditions are effective to process the melt withoutsubstantially increasing the intrinsic viscosity of the melt and whichare ineffective at promoting transesterification reactions. In somepreferred aspects, suitable operating conditions effective to establisha physical blend of the base polymer, oxidizable organic component, andtransition metal are temperatures in the melt processing zone within arange of about 250° C. to about 300° C. at a total cycle time of lessthan about 6 minutes, and typically without the application of vacuumand under a positive pressure ranging from about 0 psig (pound-force persquare inch gauge) to about 900 psig. In some embodiments, the residencetime of the melt on the screw can range from about 1 to about 4 minutes.

EXPERIMENTAL

The following examples are put forth so as to provide those of ordinaryskill in the art with a complete disclosure and description of how thecompounds, compositions, articles, devices and/or methods claimed hereinare made and evaluated, and are intended to be purely exemplary and arenot intended to limit the disclosure. Efforts have been made to ensureaccuracy with respect to numbers (e.g., amounts, temperature, etc.), butsome errors and deviations should be accounted for. Unless indicatedotherwise, parts are parts by weight, temperature is in ° C. or is atambient temperature, and pressure is at or near atmospheric.

Example 1 Synthesis of 1,3,5-Tris(phthalimidinomethyl)benzene

A mixture of 61.1 g (459 mmol) of phthalimidine, 42.9 g (120 mmol) of1,3,5-tris(bromomethyl)benzene and 177.1 g (544 mmol) of Cs₂CO₃ in 1 Lof CH₃CN was refluxed for 19 hours. After cooling to room temperature,the reaction mixture was partitioned between 1 L of EtOAc and 1 L ofdeionized water and the phases were separated. The organic phase waswashed with 802 g of brine and dried over 203 g of anhydrous Na₂SO₄. Theliquid was decanted from the drying agent and the drying agent wasslurried in 500 ml of CH₂Cl₂ to try to dissolve some insoluble brownsolid that remained. The combined organic phases were concentrated invacuo to yield 74.1 g of orange solid. TLC (EtOAc) showed this materialto be a mixture of the desired product and starting phthalimidine.

The crude material was dissolved in 200 ml of CH₂Cl₂ @ 35° C. Half ofthis was chromatographed over 1163 g of silica gel (70-230 mesh),eluting with EtOAc. After a forerun of 1.3 L, 70×250 ml fractions werecut. Pure product fractions were pooled and concentrated in vacuo. Thesecond half of the crude solution was chromatographed similarly andproduct fractions combined with those from the first run. The yield,after collection and drying in vacuo to constant weight, was 8.6 g.

The second column was washed exhaustively with EtOAc in the suspicionthat the product, with limited solubility in EtOAc, had crystallized onthe column and was being slowly eluted off. Washing the column with 4.5L of EtOAc gave another 4.0 g of product.

The reaction scheme is depicted below:

Example 2

The compound, DCX-600 prepared in Example 1{1,3,5-Tris(phthalimidinomethyl) benzene OR[1,3,5-phenylenetris(methylene)]tris-[2,3-dihydro-1H-Isoindol-1-one]}was mixed at 1.4 wt % with hot, dry PET resin (Vitiva™ from EastmanChemical Company) and 80 ppm Cobalt catalyst (added as a PET basedmasterbatch). This mixture was fed into BOY 22S injection moldingmachine to mold plaques. To compare the O₂ scavenging performance ofDCX-600, plaques made with DC-300 (LDR=1.4 wt %) were also molded at thesame time, under similar processing conditions. These plaques wereground up and analyzed for O₂ scavenging performance using Oxysense™.FIG. 1 shows the Oxysense data for compound DCX-600 as a function oftime. As seen from FIG. 1, plaques made using DCX-600 compound in PETscavenged oxygen at a rate similar to DC-300 at 75 C.

Example 3

The compound 2-benzyl-1-isoindolinone (DCX-300-1) was prepared byreacting benzyl amine with phthalide (2-benzofuran-1(3H)-one. Thechemical structure of 2-benzyl-1-isoindolinone is shown below:

1.4 weight % of this compound DCX-300-1 (lot number LP 081710, preparedby Cymer LLC, Decatur, Tenn.) was mixed with dried Eastlon CB-651S (lotnumber 0104896, manufactured by Far Eastern Textiles) resin and 80 ppmcobalt catalyst (added as a solid masterbatch of Cobalt Neodecanoate inPET). The PET resin was dried in a Piovan dryer at 170 C for 4 hoursbefore being used for mixing. The mixture was fed into the BOY 22 Sinjection molding machine to mold plaques. The BOY 22 S injection molderbarrel temperatures during injection molding was ˜275° C. for bothheating zones, the injection pressure was ˜700 psi, nozzle heater andsprue heater temperatures were ˜280° C. The mold was water cooled. Theplaques were tested for oxygen scavenging using Oxysense™. The Oxysense™data is shown in FIG. 2. As seen from FIG. 2, the di-functional O₂scavenger (DCX-300-1) scavenges O₂ at a rate similar to that for ConstarInternational's DC-300 oxygen scavenger (tetra-functional O2 scavenger)

It will be apparent to those skilled in the art that variousmodifications and variations can be made in the present inventionwithout departing from the scope or spirit of the invention. Otherembodiments of the invention will be apparent to those skilled in theart from consideration of the specification and practice of theinvention disclosed herein. It is intended that the specification andexamples be considered as exemplary only, with a true scope and spiritof the invention being indicated by the following claims.

What is claimed is:
 1. A compound having a structure of Formula III orFormula IV:

wherein the symbol - - - when used in conjunction with a bond linerepresents a single or a double bond; wherein each n of Formula III isindependently 1-5; wherein each n of Formula (IV) is independently 2-5;wherein m is an integer from 0 to 5-n; wherein each X is independentlyselected from the group consisting of O, S, and NH; wherein each Y, eachA, and each B are independently selected from the group consisting of N,CR¹, and CR²; wherein D, E, and F are independently selected from thegroup consisting of CH, N, O, and S; wherein each R¹ and each R² isindependently selected from the group consisting of H, alkyl, aryl,electron withdrawing groups, electron releasing groups, and a transitionmetal; and wherein L is a divalent linking group selected from C2-C12aliphatic or cyclic ether, C2-C12 aliphatic or cyclic amide, C6 to C12aromatic amide, C2-C12 aliphatic or cyclic amine, C6-C12 aromatic amine,C2-C12 aliphatic or cyclic ester and C6 to C12 aromatic ester.
 2. Thecompound of claim 1, wherein m is
 0. 3. The compound of claim 1, whereineach X is O.
 4. The compound of claim 1, wherein each Y, each A, andeach B are CR¹.
 5. The compound of claim 1, wherein each Y, each A, andeach B are CH.
 6. The compound of claim 1, wherein D, E, and F are CH.7. The compound of claim 1, wherein L is selected from:

wherein R is a divalent organic residue selected from alkyl, alkenyl,alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, cycloalkyl,cycloalkenyl, cycloalkynyl, heterocycloalkyl, heterocycloalkenyl,heterocycloalkynyl, aryl, and heteroaryl, and wherein R has from 1 to 8carbons; and wherein each R′ is independently C1-C6 alkyl.
 8. Thecompound of claim 1, having a structure:


9. The compound of claim 8, having a structure:


10. The compound of claim 8, having a structure:


11. The compound of claim 8, having a structure:


12. The compound of claim 1, having a structure:


13. The compound of claim 12, having a structure:


14. The compound of claim 12, having a structure:


15. The compound of claim 12, having a structure: